Targeting the HIF2-VEGF axis in renal cell carcinoma.
review · Level V
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- Record sourced from PubMed, PMID 33020645.
- Also identified by DOI 10.1038/s41591-020-1093-z.
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Abstract
Insights into the role of the tumor suppressor pVHL in oxygen sensing motivated the testing of drugs that target the transcription factor HIF or HIF-responsive growth factors, such as VEGF, for the treatment of cancers caused by VHL inactivation, such as clear-cell renal cell carcinoma (ccRCC). Multiple VEGF inhibitors are now approved for the treatment of ccRCC, and a HIF2α inhibitor has advanced to phase 3 development for this disease. These inhibitors are now also increasingly combined with immune-checkpoint blockers. In this Perspective, we describe the understanding of the mechanisms of oxygen sensing and hypoxia signaling that resulted in the development of HIF2α-targeted therapies for patients with VHL-associated tumors. We also present future directions for extending the use of these therapies to other cancers.
Medical subject headings
- Antineoplastic Agents
- Basic Helix-Loop-Helix Proteins
- Carcinoma, Renal Cell
- Kidney Neoplasms
- Molecular Targeted Therapy
- Vascular Endothelial Growth Factor A